The UMD-MSH2 mutations database
Mutation c.478_479delCA

     Data for this mutation

Co occurence of MLH1, MSH2, MSH6, MUTYH and APC mutations (Pathogenic mutations, Unclassified variants, Non-pathogenic variation)

Sample ID	MSH2	MLH1	MSH6	MUTYH	APC
19_15011_15011-001_15011-	-	-	-	-	-

Biological significance	Date	Comment
Causal	21/02/14	---